OBO ID: DOID:0111146 |
Term Name: | acquired von Willebrand syndrome | Search Ontology: | |
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Definition: | A blood coagulation disease characterized by development of a defect in clotting in the absence of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age. Typically this develops secondarily to other disorders, such as lymphoproliferative, myeloproliferative, cardiovascular and autoimmune disorders. https://www.ncbi.nlm.nih.gov/pubmed/28028990 | ||
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Ontology: | Human Disease ( DOID:0111146 ) |
OTHER acquired von Willebrand syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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